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NCT07137338 · ClinicalTrials.gov registry record · Phase 1

A Phase 1 AAV Gene Therapy Trial Evaluating Safety and Preliminary Efficacy of RP-A701 in Subjects With BAG3 Dilated Cardiomyopathy

A Phase 1 study, sponsored by Rocket Pharmaceuticals.

Recruiting
Registry status
Phase 1
Development phase
8
Enrollment target

NCT07137338: Recruiting Phase 1 study, sponsored by Rocket Pharmaceuticals.

NCT07137338 is a Phase 1 study that is actively recruiting participants, run by Rocket Pharmaceuticals. The registered enrollment target is 8 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (87% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07137338, a Phase 1 study, is actively recruiting participants, sponsored by Rocket Pharmaceuticals.

RECRUITING
Registry status
Phase 1
Development phase
8 participants
Enrollment target

Study Summary

This is a Phase 1, open-label, dose-escalation trial to characterize the safety, tolerability, and preliminary efficacy of RP-A701 following a single IV administration in high-risk adult patients with BAG3-DCM.

Primary Outcome

Number of participants with Adverse Events following a single IV dose of RP-A701

Interventions

  • GENETIC RP-A701 is a recombinant viral vector composed of an AAV serotype rh.74 (AAVrh.74) capsid encapsulating the transgene, BCL2-associated Athanogene 3 (BAG3)

Trial Details

FieldValue
Enrollment Target 8 participants
Start Date 2026-06
Est. Completion 2029-06
Phase Phase 1
Rocket Pharmaceuticals

10 total trials

What NCT07137338 shows while recruiting

NCT07137338 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 8 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (87% lower).

The record links to 0 conditions, and to 1 intervention - of which RP-A701 is a recombinant viral vector composed of an AAV serotype rh.74 (AAVrh.74) capsid encapsulating the transgene, BCL2-associated Athanogene 3 (BAG3) is the first listed.

NCT07137338 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT07137338 about?

NCT07137338 is a clinical study titled "A Phase 1 AAV Gene Therapy Trial Evaluating Safety and Preliminary Efficacy of RP-A701 in Subjects With BAG3 Dilated Cardiomyopathy". This is a Phase 1, open-label, dose-escalation trial to characterize the safety, tolerability, and preliminary efficacy of RP-A701 following a single IV administration in high-risk adult patients with BAG3-DCM.

What is the current status of trial NCT07137338?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 8 participants. The study started on 2026-06. Estimated completion is 2029-06.

What interventions are being tested in trial NCT07137338?

The interventions under investigation include: RP-A701 is a recombinant viral vector composed of an AAV serotype rh.74 (AAVrh.74) capsid encapsulating the transgene, BCL2-associated Athanogene 3 (BAG3) (GENETIC).

Who is sponsoring clinical trial NCT07137338?

This trial is sponsored by Rocket Pharmaceuticals, which has 10 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT07137338's enrollment target sits among peer trials

8 1959th of 2000 higher than 29 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT07137338, the US trial registry maintained by the National Library of Medicine. NCT07137338 (small enrollment · none site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.